What Is the Objective and Benefits of TL 9000 Certification?

In 1998 Journey Gathering (a gathering of specialist organizations, providers, what's more, contacts devoted to Telecom industry) built up the TL 9000 Quality Administration Framework to meet the store network quality prerequisites of the overall media communications industry.

TL 9000 means to accomplish the accompanying objectives:

•Establish and keep up a typical arrangement of telecom QMS prerequisites, which diminishes the quantity of gauges for the business

•Foster a framework that ensures the honesty and utilization of telecom items equipment, programming and administrations

•Define viable cost and execution based estimations to control advance and assess the consequences of QMS implementation

•Drive ceaseless change and upgrade client connections

•Leverage the business congruity evaluation process

Particular Prerequisites for Broadcast communications

The TL 9000 Certification standard is the telecom business' augmentation to ISO 9001 and incorporates supplemental prerequisites in the accompanying zones:

•Performance estimations in view of unwavering quality of item

•Software improvement and life-cycle administration

•Requirements for particular administration capacities, for example, establishment and designing

•Requirements to address interchanges between telecom organize administrators and providers

•Reporting of value estimation information to a focal vault

TL 9000 Consistence

A two-section quality framework with critical administration and estimation parts, TL 9000 enlisted associations are required to agree to:

•All prerequisites statements of the Universal Benchmarks ISO 9001:2000

•Telecom-particular prerequisites that apply to all enlistments

•Telecom-particular prerequisites that apply to equipment, programming or potentially benefit enlistments

•Telecom industry estimations that apply in all item classifications

•Telecom industry estimations that apply in certain item classifications particular to equipment, programming and additionally benefits

Who Advantages from TL 9000?

•Buyers advantage from guaranteed reliable quality over all items and administrations by utilizing TL 9000 confirmed providers, alongside critical cost investment funds of on location reviews.

•Suppliers benefit by conformance to TL 9000 gauges, hence approving the nature of item, administrations and client mind that they give. It diminishes the expenses of value reviews and makes tweaked execution reports for present and potential clients.

•Both Specialist co-ops and Providers pick up from cost efficiencies and enhanced provider connections over the production network.

•Organizations drive facilitates item and administration change through a solid sense of duty regarding quality and business perfection, in this way boosting their opportunity to-showcase and upper hand.

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HOW TO GET HACCP CERTIFICATION - HAZARD ANALYSIS CRITICAL CONTROL POINT?

IAS provide comprehensive support for creating and implementing a suitable HACCP (Hazard Analysis Critical Control Point), which is an internationally accepted standards for preventing microbiological, chemical and physical contamination, along the food supply chain. A HACCP standard is designed to provide increased control and monitoring during critical stages of the food processing chain.

Food safety management system should allow you to identify and control any hazards that could pose a danger to the preparation of safe food. It involves identifying and forecasting what can go wrong, planning to prevent it and making sure you are doing it. HACCP is a legal requirement but will also benefit your business.

WHO CAN APPLICABLE FOR HACCP?

·         Fruits & Vegetables

·         Dairy Products

·         Meat & Meat Products

·         Farms, Fish & Fishery Products

·         Nuts & Nut Products

·         Bakery & Confectionary

·         Restaurants &• Hotels

·         Fast Food Operations etc.

BENEFITS OF HACCP CERTIFICATION

·         Improved food safety management system

·         Increased awareness of food risks to employees.

·         Increased customers and consumer confidence

·         Consistency in inspection process.

·         Commitment to legal Compliance with food law

·         Reduction in complaints about food safety

·         Reduced risk of negative publicity

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WHAT ARE THE FEATURES OF ISO/TS 16949 CERTIFICATION?

We provide a auditing services in the latest version of ISO/TS 16949, 3rd Edition published in June 2009, Standard is for automotive industry Quality Management System (QMS). ISO/TS 16949:2008 was introduced and developed by IATF (International Automotive Task Force) members and aligned by ISO (International Organization for Standardization) for publication.

As being an extended version and with MORE CONTROLS of ISO 9001:2008 quality management system. IAS provides value added audits as specified in the QMS for the design/development, production, and installation and servicing of automotive-related products. IAS ensures that the Organization is more focused implementing such system in place to provide harmonized quality systems within the automotive supply chain, resulting in a focused and consistent approach.

IAS auditors with vast experience shall provide practically value added audits which enhances the organization’s ability to create and maintain a robust system in order to provide more consistency in output through which customers are happier and also brings in new customers for the organization.

KEY FEATURES OF ISO/TS 16949 STANDARD CERTIFICATION

·         Quality improvement in product & process.

·         Confidence to the customers.

·         Common approach for managing Quality Management System

·         Reassignment of resources to quality improvement and

·         Reduction in the multiple 3rd party registrations.

BENEFITS OF ISO/TS 16949CERTIFICATION

·         Help you to do business worldwide.

·         Reduces waste and prevents defects

·         Flexible and easy to adopt

·         Reduced operating costs

·         Improved stakeholder relationships

·         Specify the Legal compliance

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WHAT ARE THE BENEFITS OF ISO 10002 CERTIFICATION?

Customer satisfaction is key to any business. One way to improve your customer satisfaction is by identifying and eliminating the dissatisfaction causes hidden in your system. This complaint management system helps your organization to handle the customer complaints more systematically and improve the satisfaction index.

The system helps the organization to identify the cause(s).

Find the expectations of your customers.

Monitor and continually improve the complaint resolving systems.

IAS audits and provides certification for this standard ISO 10002 Certification as per the IAS audit procedure.

BENEFITS OF ISO 10002

There are various advantages to actualizing and affirming your client dissensions administration framework:

Client maintenance:

By embracing the administration framework, your capacity to hold the devotion of your clients will be upgraded.

Brand notoriety:

Executing and guaranteeing your protests administration framework exhibits to partners that you have a genuine responsibility regarding overseeing client mind issues and you have forms set up to deal with, dissect and survey grievances.

Operational proficiency:

Usage and affirmation guarantees a predictable way to deal with taking care of client questions, empowering you to distinguish drifts and dispose of the reasons for objections, and enhance your association's operations.

Enhanced inward correspondences and relations:

It causes you to embrace a client cantered way to deal with settling objections and urge faculty to enhance their abilities in working with clients.

Adaptability:

The standard is perfect with ISO 9001 Quality enabling you to add esteem and productivity to your association. ISO 10002 Certification Provider - add A likewise gives direction particularly to private companies.

Ceaseless change:

It gives a premise to ceaseless survey and examination of your grievances taking care of process, the determination of dissensions and where upgrades can be made.

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Our friendly training team will assist you and answer any questions you may have. Please contact us on +91 9566117567, 8220666148, 9600051938 or via email:info@iasiso.com

HOW TO GET ISO 13485 CERTIFICATION FOR MEDICAL DEVICES?

ISO 13485 is an international standard for the design, manufacture and distribution of medical devices. ISO 13485:2012 is the latest version by ISO.  This standard is based on the ISO 9001:2008 process model approach.

ISO 13485 certification process based approach which define, implement, and improve effectives of quality management system that they expected by customers and regulatory requirements. The main aim of ISO 13485:2012 is to facilitate harmonized medical device regulatory requirements for quality management systems.

ISO 13485 Certification is closely aligned to other management standards such as ISO 9001, ISO 14001 and OHSAS 18001 providing a great opportunity for integration and synergy with other quality systems.

BENEFITS OF IMPLEMENTING ISO13485 STANDARDS:

The main internal benefits of 13485 standard is that it indicate a preventive approach to assuring medical device quality which the process inspection and rejection are done at the end of the manufacturing line.

·       Its provides a systematic framework for to define, implement, measure and analyze the process of business operation and customer opinion.

·    It provides a systematic framework on monitored base that resulting in less waste and fewer complaints.

·     Reduction of operating costs, reduction of nonconforming products costs, raw materials, energy and other resources saving.

·         This standard focused to improve the performance in areas such as sales, product delivery, and process efficiency.

·         Its reduce costs as a result of minimizing product failures.

·       Through ISO 13485 standard organization access to the competitive edge with our independently. 

NEED MORE INFORMATION About ISO Certification?

Our friendly training team will assist you and answer any questions you may have. Please contact us on +91 9566117567, 8220666148, 9600051938 or via email :info@iasiso.com

HOW TO GET ISO 50001 CERTIFICATION FOR ENERGY MANAGEMENT SYSTEM?

ISO 50001:2011 is a first standard for energy management system published by ISO on June 2011. ISO 50001 has provides structured framework for organizations to manage and control energy that it can increase energy efficiency, reduce costs and improve energy performance. ISO 50001 is intended to help business make better use of your energy consumption or energy performance through a systematic approach. 

The standard is compatible with other management system especially ISO 14001 (Environmental Management System) and ISO 9001 (Quality Management System). ISO 50001 certification Body is based on the Plan-Do-Check-Act (PDCA) cycle and it integrates to works both the technical and managerial activities.

KEY FEATURES OF ENERGY MANAGEMENT SYSTEM

·         The standard has defines your energy policy, objective and targets that relate to use of energy.

·         Continual improvement in the energy performance

·         Its Create transparency and facilitate communication on the management of energy resources and promotion of energy.

·         Periodically review the energy use, consumption and efficiency.

·         Prioritization of issues affecting energy use and efficiency

·         Its reduce the costs and Green House Gas (GHG) emissions.

·         Formalizing control systems and monitoring processes has works based on PDCA cycle.

·         Evaluation of compliance with legal and other requirements.

BENEFITS OF ACHIEVING ISO 50001 STANDARD

·         ISO 50001 standards have clearly specify the requirements of energy management of organization.

·         Its help to frame the opportunities for to improve the energy management.

·         Continually improve energy management.

·         Reduces the carbon emissions and other environmental collision.

·         Its create loyalty to business that it can increase the customer and shareholders. 

Get a enquiry For ISO 50001 certification

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Our friendly training team will assist you and answer any questions you may have. Please contact us on +91 9566117567, 8220666148, 9600051938 or via

email :training@iasiso.com

WHAT ARE THE BENEFITS ISO 13485 INTERNAL AUDITOR?

ISO 13485 outlines quality management system requirements for design, development, production and servicing of medical devices and related services. Get to grips with the entire internal auditing process, learn to plan audits, report on results and lead on follow up action.

WHAT ARE THE BENEFITS TO YOU?

This course will give you a good understanding of how to perform an internal audit on your organisation's processes. This will help you and your organisation to identify gaps in your quality management system as a basis for improvement of regulatory compliance and system effectiveness. Our experienced auditors will also guide you through ISO 13485:2003 so that you have a good understanding of what your certification body is looking for the next time they audit you.

APPLIED- PRACTICAL TRAINING…

We have developed our training courses to make them hands on and interactive. Simply put, it is our belief that if we keep you involved in learning you will learn more and be able to use more back at work.

SELF-POSSESSION THAT YOUR QUALIFICATION IS VALID…

As an IRCA approved training course, this course, our company and our trainers undergo an intensive inspection and assessment every year with the International Register of Certificated Auditors (IRCA) to give you the peace of mind that your qualification is valid and will be recognised by your customers and certification body.

HOW TO BOOK…

Our course calendar can be viewed below or just go to our BOOK NOW page if you know the course date you require. Not too sure about which course to book? Just call us on 9566117567   to discuss your training needs further

PRE-REQUIREMENTS

This course is intended for those responsible for audit program for ISO 13485:2003, for those who perform the audit, for Quality Assurance managers, ISO Project Managers, ISO Project Team Members and for Managers & Supervisors interested in deeper understanding of ISO 13485 Internal Auditor Training and its practical application.

ON THE COURSE COMPLETION PARTICIPANTS WILL LEARN HOW TO

·         interpret & apply the requirements of ISO 13485

·         use the QMS and ISO 13485 training Course to ensure compliance to applicable regulations

·         identify & implement the controls necessary for ensuring that QMS consistently meets requirements.

·         conduct audit.

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ISO 17025 INTERNAL AUDITOR TRAINING

ISO17025 internal Auditor Training people who are willing to be certified lead auditor for ISO-17025. ISO-17025 organization of the work of internal audit staff, develop their own lab management and test operations, enabling them to comply with the ISO-17025. Upon completing the course and take the exam, candidates receive certification.

THE BACKGROUND

In ISO is a large international organization, the origin and dissemination of international standards, international quality products, systems and services for supervision. Standard ISO-17025 laboratory use their laboratory system and the structure of the program. In addition, a barometer of the regulatory and certification bodies using standard laboratory proficiency testing.

THE CHARACTERISTICS

Internal auditor training courses to teach candidates how to set and how to evaluate audit results and take corrective measures and coordination of audit. Corrective action by the internal audit staff, to help laboratories to make the necessary changes before the formal review of the regulatory bodies and certification bodies.

IDENTIFICATION

ISO-17025internal auditor course is for individuals who wish to be certified as an ISO-17025 internal auditor. ISO-17025 internal auditors work for organizations looking to develop their laboratory management and testing operations so they comply with ISO-17025. Upon completing the coursework and taking the exam, candidates receive a certification.

BACKGROUND

The ISO is a large international organization that originates and publishes international standards to oversee the quality of products, systems and services internationally. ISO-17025 is the standard that laboratories use to structure their laboratory systems and procedures. In addition, regulatory and accreditation agencies use the standard as a barometer to validate the competence of laboratories.

FEATURES

Internal auditor training programs teach candidates how to set up and coordinate an audit as well as how to evaluate audit findings and implement corrective action. Internal auditors use corrective action to help the laboratories make the necessary changes prior to a formal audit from regulatory agencies and accreditation organizations.

On training completion you will be able to:

·         Understand the requirements of ISO/IEC 17025:2005

·         Understand the principles of testing and calibration

·         Learn how to plan, prepare, conduct, report and follow up an internal audit

·         Understand how to apply the framework for any type of laboratory, company or culture Participants are expected to possess knowledge of auditing, laboratory management systems and ISO/IEC 17025 before attending the training.

Contact IAS now to find out more on IAS ISO/IEC 17025 Internal Auditor Training.

WHO SHOULD ATTEND?

·         Individuals wishing to perform internal laboratory audits

·         Laboratory Managers and Supervisors

·         Companies seeking ISO/IEC 17025 accreditation

·         Registrar/Accreditation body Auditors

·         Existing internal auditors who are looking to expand their skills in the area of laboratory practices

·         Supplier Quality Auditors wishing to evaluate laboratory service suppliers, including calibration suppliers

BOOKING AND COURSE FEES

FEES INCLUDED

·         Delegate workbook, including reference information.

·         Training provided by qualified and experienced tutors with extensive practical management auditing experience across a variety of manufacture and service industries.

·         Refreshments during the day.

·         Certificate verifying attendance and completion of course

NEED MORE INFORMATION About ISO Certification and Training?

Our friendly training team will assist you and answer any questions you may have. Please contact us on +91 9566117567, 8220666148, 9600051938 or via email:training@iasiso.com